Effect of cucurbitacins on bilirubin–albumin binding in human plasma

• Published in: Life sciences (1973) Vol. 80; no. 6; pp. 579 - 585
• Main Authors: Greige-Gerges, H., Abou Khalil, R., Chahine, R., Haddad, C., Harb, W., Ouaini, N.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 16-01-2007
• Subjects: Albumin; Bilirubin; Bilirubin - blood; Bilirubin - metabolism; Cucurbitacin; Dose-Response Relationship, Drug; Human plasma; Humans; Hyperbilirubinemia - blood; Hyperbilirubinemia - metabolism; Protein Binding - drug effects; Serum Albumin - metabolism; Triterpenes - pharmacology; Albumin; Cucurbitacin; Human plasma; Bilirubin
• ISSN: 0024-3205; 1879-0631
• DOI: 10.1016/j.lfs.2006.10.005

The aim of this study is to investigate the effect of three cucurbitacins (Cuc) E, D and I on the bilirubin–albumin binding, both in human serum albumin (HSA) and in plasma. Bilirubin–HSA solution and plasma free of cucurbitacins were prepared as well as others containing serial concentrations of cucurbitacins. The concentration of unbound bilirubin was determined in bilirubin–HSA solution and the direct and total bilirubin concentrations were measured in plasma (with normal or elevated bilirubinemia) by Jendrassik and Grof method. In the conditions we adopted Cuc E and D (to a lesser extent), decreased the levels of unbound bilirubin in bilirubin–HSA solution and decreased direct bilirubin concentration and total bilirubin concentration in plasma in a dose-dependent manner while Cuc I had no effect. The effect of Cuc is related to the presence of native HSA. Thus, when albumin was absent or has been denatured by heating or by urea, Cuc E did not modify bilirubin levels, suggesting that the native structure of albumin is essential for such activity. The interaction of HSA with Cuc E was investigated by fluorescence spectroscopy. Cuc E increased the intrinsic fluorescence of the protein and the magnitude of fluorescence intensity of bilirubin–albumin complex. We concluded that Cuc E and D produced a rearrangement in the structure of albumin, particularly in the domain-II, resulting in an increase in the binding of bilirubin to albumin regardless to whether it's conjugated to glucuronic acid or unconjugated.